JP2017508858A5 - - Google Patents
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- JP2017508858A5 JP2017508858A5 JP2016572913A JP2016572913A JP2017508858A5 JP 2017508858 A5 JP2017508858 A5 JP 2017508858A5 JP 2016572913 A JP2016572913 A JP 2016572913A JP 2016572913 A JP2016572913 A JP 2016572913A JP 2017508858 A5 JP2017508858 A5 JP 2017508858A5
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- resin composition
- weight
- composition according
- photocurable
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000000203 mixture Substances 0.000 claims description 21
- 239000003211 photoinitiator Substances 0.000 claims description 5
- 230000003014 reinforcing Effects 0.000 claims description 5
- 239000002318 adhesion promoter Substances 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims 22
- 229920000647 polyepoxide Polymers 0.000 claims 22
- 125000003700 epoxy group Chemical group 0.000 claims 5
- GYZLOYUZLJXAJU-UHFFFAOYSA-N Diglycidyl ether Chemical group C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims 4
- 239000011258 core-shell material Substances 0.000 claims 4
- 229920001971 elastomer Polymers 0.000 claims 4
- 229910052751 metal Inorganic materials 0.000 claims 4
- 239000002184 metal Substances 0.000 claims 4
- 229920005862 polyol Polymers 0.000 claims 4
- 239000005060 rubber Substances 0.000 claims 4
- 239000004593 Epoxy Substances 0.000 claims 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- -1 ether polyol Chemical class 0.000 claims 3
- MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical class [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 claims 3
- 229920000570 polyether Polymers 0.000 claims 3
- 150000003077 polyols Chemical class 0.000 claims 3
- PXKLMJQFEQBVLD-UHFFFAOYSA-N Bis(4-hydroxyphenyl)methane Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 claims 2
- IISBACLAFKSPIT-UHFFFAOYSA-N Bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims 2
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N Bisphenol S Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims 2
- 239000005062 Polybutadiene Substances 0.000 claims 2
- 239000004793 Polystyrene Substances 0.000 claims 2
- 125000002091 cationic group Chemical group 0.000 claims 2
- 238000006056 electrooxidation reaction Methods 0.000 claims 2
- 229920003986 novolac Polymers 0.000 claims 2
- 229920002857 polybutadiene Polymers 0.000 claims 2
- 229920002223 polystyrene Polymers 0.000 claims 2
- 238000007789 sealing Methods 0.000 claims 2
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical class [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims 2
- XUCHXOAWJMEFLF-UHFFFAOYSA-N 2-[[4-[[4-(oxiran-2-ylmethoxy)phenyl]methyl]phenoxy]methyl]oxirane Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 claims 1
- HVAFEPYLJVNTJL-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;oxetane Chemical compound C1COC1.CCC(CO)(CO)CO HVAFEPYLJVNTJL-UHFFFAOYSA-N 0.000 claims 1
- JOLVYUIAMRUBRK-UTOQUPLUSA-N 3-[(8Z,11Z)-pentadeca-8,11,14-trienyl]phenol Chemical compound OC1=CC=CC(CCCCCCC\C=C/C\C=C/CC=C)=C1 JOLVYUIAMRUBRK-UTOQUPLUSA-N 0.000 claims 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 claims 1
- LJQLCJWAZJINEB-UHFFFAOYSA-N Hexafluorophosphate Chemical compound F[P-](F)(F)(F)(F)F LJQLCJWAZJINEB-UHFFFAOYSA-N 0.000 claims 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 claims 1
- 229920000451 Polycaprolactone-block-polytetrahydrofuran-block-polycaprolactone Polymers 0.000 claims 1
- 239000004902 Softening Agent Substances 0.000 claims 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 229920001400 block copolymer Polymers 0.000 claims 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims 1
- 150000007942 carboxylates Chemical group 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims 1
- 150000002009 diols Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 150000002191 fatty alcohols Chemical class 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 239000011521 glass Substances 0.000 claims 1
- MBAKFIZHTUAVJN-UHFFFAOYSA-H hexafluoroantimony(1-) Chemical compound F[Sb-](F)(F)(F)(F)F MBAKFIZHTUAVJN-UHFFFAOYSA-H 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 239000011159 matrix material Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 150000002921 oxetanes Chemical class 0.000 claims 1
- 229920001610 polycaprolactone Polymers 0.000 claims 1
- 239000004632 polycaprolactone Substances 0.000 claims 1
- 229920000728 polyester Polymers 0.000 claims 1
- 229920005906 polyester polyol Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 229920000909 polytetrahydrofuran Polymers 0.000 claims 1
- 239000003566 sealing material Substances 0.000 claims 1
- 150000004756 silanes Chemical class 0.000 claims 1
- 125000005409 triarylsulfonium group Chemical group 0.000 claims 1
- 150000004072 triols Chemical class 0.000 claims 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
Description
本発明による組成物を調製するために、ベース樹脂および強化剤を攪拌機中で真空下、室温でブレンドした。軟化剤および、場合により、反応性希釈剤を混合物に添加し、再度真空下で撹拌した。次に、光開始剤を添加し、真空下で撹拌した。接着促進剤を添加した場合、これは最終工程で添加し、混合物を再度室温、真空下で混合した。 To prepare the composition according to the invention, the base resin and the toughening agent were blended in a stirrer under vacuum at room temperature. Softener and optionally reactive diluent was added to the mixture and again stirred under vacuum . Next, the photoinitiator was added and stirred under vacuum . If an adhesion promoter was added, it was added in the final step and the mixture was again mixed at room temperature under vacuum .
製造したフィルムは、軟化剤および補強助剤を用いない場合、柔軟性および靱性が低下することを示す。ここで、高い柔軟性および靱性は、軟化剤または軟化剤と補強助剤との組み合わせのいずれかの影響下において得ることができる。光開始剤UV-2257の使用は、再度、より高い靱性を有する比較的より柔軟性のフィルムをもたらす。 The produced film shows a decrease in flexibility and toughness when softeners and reinforcing aids are not used. Here, high flexibility and toughness can be obtained under the influence of either a softener or a combination of a softener and a reinforcing aid. Use of a photoinitiator UV-2257 again, resulting in relatively more flexible film to have a higher toughness.
Claims (14)
(b)2〜30重量%、好ましくは5〜15重量%の、強化剤としての少なくとも1つのコア-シェルゴム;
(c)1〜20重量%、好ましくは5〜10重量%の、エポキシ基、カルボキシレート基、アミノ基および/またはヒドロキシル基の中から選択される反応性官能基を含む少なくとも1つの軟化剤;および
(d)1〜4重量%、好ましくは1.5〜2.5重量%の、少なくとも1つのカチオン性光開始剤、好ましくはスルホニウム塩および/またはヨードニウム塩を含むカチオン性光開始剤
を含む光硬化性エポキシ樹脂組成物。 (A) 30 to 90% by weight, preferably 50 to 85% by weight of at least one aromatic epoxy resin;
(B) 2-30% by weight, preferably 5-15% by weight of at least one core-shell rubber as reinforcing agent;
(C) 1 to 20% by weight, preferably 5 to 10% by weight of at least one softener comprising a reactive functional group selected from among epoxy groups, carboxylate groups, amino groups and / or hydroxyl groups; And (d) 1-4% by weight, preferably 1.5-2.5% by weight of at least one cationic photoinitiator, preferably a cationic photoinitiator comprising a sulfonium salt and / or an iodonium salt Photocurable epoxy resin composition.
(i)好ましくは0.1〜10重量%、特に好ましくは0.5〜2.5重量%の量の、補強助剤;および/または
(ii)好ましくは0.1〜10重量%、特に好ましくは5〜10重量%の量の、反応性希釈剤;および/または
(iii)好ましくは0.1〜3重量%、特に好ましくは0.5〜2重量%の量の、接着促進剤
も含むことを特徴とする、請求項1〜7のいずれかに記載の光硬化性エポキシ樹脂組成物。 The composition is:
(I) a reinforcing aid in an amount of preferably 0.1 to 10% by weight, particularly preferably 0.5 to 2.5% by weight; and / or (ii) preferably 0.1 to 10% by weight, in particular Reactive diluent, preferably in an amount of 5 to 10% by weight; and / or (iii) an adhesion promoter in an amount of preferably 0.1 to 3% by weight, particularly preferably 0.5 to 2% by weight. The photocurable epoxy resin composition according to claim 1, wherein the photocurable epoxy resin composition is contained.
(iii)請求項1〜11のいずれかに記載の光硬化性エポキシ樹脂組成物をフィルム形状において金属含有電線または電気接点に付与する工程;および
(iv)露光によりフィルムを硬化する工程
を含む方法。 A method for sealing a metal-containing wire or electrical contact for protection against electrochemical corrosion comprising:
(Iii) a step of applying the photocurable epoxy resin composition according to any one of claims 1 to 11 to a metal-containing electric wire or an electrical contact in a film shape; and (iv) a method of curing the film by exposure. .
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102014204265 | 2014-03-07 | ||
DE102014204265.8 | 2014-03-07 | ||
PCT/EP2015/054697 WO2015132372A1 (en) | 2014-03-07 | 2015-03-06 | Photocurable epoxy resin systems |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2017508858A JP2017508858A (en) | 2017-03-30 |
JP2017508858A5 true JP2017508858A5 (en) | 2018-04-19 |
JP6964981B2 JP6964981B2 (en) | 2021-11-10 |
Family
ID=52684212
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016572913A Active JP6964981B2 (en) | 2014-03-07 | 2015-03-06 | Photocurable epoxy resin system |
Country Status (8)
Country | Link |
---|---|
US (1) | US10508199B2 (en) |
EP (1) | EP3114161B1 (en) |
JP (1) | JP6964981B2 (en) |
KR (1) | KR102334119B1 (en) |
CN (1) | CN106062057B (en) |
CA (1) | CA2941484A1 (en) |
MX (1) | MX2016011506A (en) |
WO (1) | WO2015132372A1 (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102042190B1 (en) * | 2016-12-27 | 2019-11-07 | 삼성에스디아이 주식회사 | Photo-sensitive Composition, Cured Film Prepared Therefrom, and Electronic Device Incoporating the Cured Film |
JP2020521839A (en) * | 2017-05-25 | 2020-07-27 | ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング | Curable composition |
EP3421567A1 (en) * | 2017-06-28 | 2019-01-02 | Henkel AG & Co. KGaA | Uv pre-curable epoxide composition for two stage process of assembly |
CZ308202B6 (en) * | 2017-09-11 | 2020-02-26 | TESORO Spin off, s.r.o. | Flexible composite materials and preparing and using them |
KR102244789B1 (en) * | 2017-12-15 | 2021-04-26 | 주식회사 엘지화학 | Polarzing plate, polarizing plate-carrier film laminate, the method for manufacturing the polarizing plate and the active energy beam-cured composition for protective layer of polarizer |
KR102244791B1 (en) * | 2017-12-15 | 2021-04-26 | 주식회사 엘지화학 | Polarzing plate, polarizing plate-carrier film laminate, the method for manufacturing the polarizing plate and the active energy beam-cured composition for protective layer of polarizer |
US10858541B2 (en) * | 2017-12-19 | 2020-12-08 | Rohm And Haas Electronic Materials Llc | Curable composition |
CN107964333B (en) * | 2017-12-29 | 2020-01-17 | 中科院广州化学有限公司 | Amino-terminated reactive fluorine-containing polymer modified waterborne epoxy coating and preparation and application thereof |
WO2019153108A1 (en) * | 2018-02-06 | 2019-08-15 | 株式会社大赛璐 | Curable epoxy resin composition and cured product thereof |
CN108623726B (en) * | 2018-05-15 | 2020-10-02 | 闽江学院 | Cardanol resin for three-dimensional printing and preparation method thereof |
CN109553766B (en) * | 2018-09-28 | 2021-11-02 | 长兴材料工业(广东)有限公司 | Modified polyester polyol and preparation method and application thereof |
TWI756770B (en) * | 2019-08-07 | 2022-03-01 | 美商3M創新有限公司 | Uv curable adhesive composition and adhesive film, adhesive tape, and bonding component comprising the same |
WO2021112091A1 (en) * | 2019-12-03 | 2021-06-10 | 株式会社Adeka | Resin composition |
CN112680159B (en) * | 2020-12-28 | 2023-04-07 | 上海仁速新材料有限公司 | Ultraviolet curing epoxy adhesive and preparation method and application thereof |
CN112831302A (en) * | 2021-01-29 | 2021-05-25 | 安田信邦(厦门)电子科技有限公司 | Cationic environment-friendly semiconductor underfill adhesive and preparation method thereof |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06507664A (en) * | 1991-05-16 | 1994-09-01 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | Epoxide based adhesive |
AU661363B2 (en) * | 1992-01-22 | 1995-07-20 | Minnesota Mining And Manufacturing Company | Photoactivatable, thermally curable epoxy compositions |
US5346939A (en) * | 1993-01-25 | 1994-09-13 | Minnesota Mining And Manufacturing Company | Water curable resin compositions |
US5877229A (en) * | 1995-07-26 | 1999-03-02 | Lockheed Martin Energy Systems, Inc. | High energy electron beam curing of epoxy resin systems incorporating cationic photoinitiators |
US6482868B1 (en) * | 1998-12-31 | 2002-11-19 | 3M Innovative Properties Company | Accelerators useful for energy polymerizable compositions |
WO2005100292A1 (en) | 2004-04-19 | 2005-10-27 | Ciba Specialty Chemicals Holding Inc. | New photoinitiators |
ATE534703T1 (en) * | 2005-08-24 | 2011-12-15 | Henkel Kgaa | EPOXY COMPOSITIONS WITH IMPROVED IMPACT RESISTANCE |
US8501033B2 (en) * | 2009-03-13 | 2013-08-06 | Dsm Ip Assets B.V. | Radiation curable resin composition and rapid three-dimensional imaging process using the same |
JP2011179101A (en) * | 2010-03-04 | 2011-09-15 | Autonetworks Technologies Ltd | Corrosion inhibitor, covered wire with terminal and wire harness |
US20150045510A1 (en) * | 2012-04-02 | 2015-02-12 | Christof Braendli | Epoxy adhesive, manufacture and use thereof |
-
2015
- 2015-03-06 WO PCT/EP2015/054697 patent/WO2015132372A1/en active Application Filing
- 2015-03-06 CN CN201580011832.6A patent/CN106062057B/en active Active
- 2015-03-06 KR KR1020167027830A patent/KR102334119B1/en active IP Right Grant
- 2015-03-06 JP JP2016572913A patent/JP6964981B2/en active Active
- 2015-03-06 EP EP15710151.0A patent/EP3114161B1/en active Active
- 2015-03-06 CA CA2941484A patent/CA2941484A1/en not_active Abandoned
- 2015-03-06 MX MX2016011506A patent/MX2016011506A/en unknown
-
2016
- 2016-09-07 US US15/258,547 patent/US10508199B2/en active Active
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